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Sample GSM756977 Query DataSets for GSM756977
Status Public on Oct 07, 2011
Title INS1 control, biological rep1
Sample type RNA
 
Source name Insulinoma 832/13 INS-1 cell line
Organism Rattus norvegicus
Characteristics passage: between passages 7 and 25
cell line: Insulinoma 832/13 INS-1 cell line
treatment: scrambled
Treatment protocol COUP-TFII depletion experiments in the 832/13 INS-1 cell line were performed as described previously (Perilhou A, Tourrel-Cuzin C, Kharroubi I, Henique C, Fauveau V, Kitamura T, Magnan C, Postic C, Prip-Buus C, Vasseur-Cognet M (2008). The transcription factor COUP-TFII is negatively regulated by insulin and glucose via FoxO1 and ChREBP controlled pathways. . Mol Cell Biol 28: 6568-6579). Briefly, cells were transfected with COUP-TFII siRNA or a scrambled siRNA using a Amaxa device following manufacturer instructions.
Growth protocol The rat insulinoma 832/13 INS-1 cell line was used between passages 7 and 25. Cells were cultured at 5% CO2–95% air at 37°C in RPMI 640 medium containing 11 mM D-glucose supplemented with 10% (v/v) heat-inactivated fetal bovine serum, 100 U/ml penicillin-streptomycin, 10 mM HEPES, 1 mM sodium pyruvate (Invitrogen), and 50 μM β-mercaptoethanol (Invitrogen) (INS-1 medium).
Extracted molecule total RNA
Extraction protocol Total RNA was extracted and purified from cultured cells using the RNA-Plus reagent according to the manufacturer’s instructions (Q-BIOgene).
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol starting from 1 ug total RNA (Expression Analysis Technical Manual, 701025 Rev5, Affymetrix).
 
Hybridization protocol Following fragmentation, 15 ug of cRNA was hybridized for 16 hr at 45C on 230 2.0 rat Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
Scan protocol GeneChips were scanned using the affymetrix 3000 genescanner
Data processing The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was set to 150
 
Submission date Jul 08, 2011
Last update date Oct 07, 2011
Contact name Leentje Van Lommel
Organization name KULeuven
Department Molecular cell biology
Lab gene expression unit
Street address Herestraat 49 bus 901
City Leuven
ZIP/Postal code 3000
Country Belgium
 
Platform ID GPL1355
Series (1)
GSE30526 COUP-TFII Controls Mouse Postnatal Pancreatic β-Cell Mass through GLP-1 β-Catenin

Data table header descriptions
ID_REF
VALUE Signal
ABS_CALL indicating whether the transcript was present (P), absent (A), or marginal (M)
DETECTION P-VALUE

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
AFFX-BioB-5_at 184.943 P 0.000224668
AFFX-BioB-M_at 250.705 P 4.42873e-05
AFFX-BioB-3_at 196.327 P 4.42873e-05
AFFX-BioC-5_at 469.237 P 5.16732e-05
AFFX-BioC-3_at 511.098 P 4.42873e-05
AFFX-BioDn-5_at 996.896 P 7.00668e-05
AFFX-BioDn-3_at 2273.13 P 7.00668e-05
AFFX-CreX-5_at 6997.88 P 4.42873e-05
AFFX-CreX-3_at 9251.09 P 4.42873e-05
AFFX-DapX-5_at 8.67062 A 0.41138
AFFX-DapX-M_at 15.8005 A 0.39692
AFFX-DapX-3_at 3.27 A 0.737173
AFFX-LysX-5_at 1.16047 A 0.52976
AFFX-LysX-M_at 2.03852 A 0.876428
AFFX-LysX-3_at 3.89747 A 0.425962
AFFX-PheX-5_at 0.621862 A 0.957038
AFFX-PheX-M_at 0.933149 A 0.937071
AFFX-PheX-3_at 3.73987 A 0.603089
AFFX-ThrX-5_at 1.96296 A 0.760937
AFFX-ThrX-M_at 1.65018 A 0.529762

Total number of rows: 31099

Table truncated, full table size 947 Kbytes.




Supplementary file Size Download File type/resource
GSM756977_A13wt.CEL.gz 2.3 Mb (ftp)(http) CEL
GSM756977_A13wt.CHP.gz 170.0 Kb (ftp)(http) CHP
Processed data included within Sample table

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